A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9938n54



Internal ID22777833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97669437..97772855hg38UCSC Ensembl
chr5:97005141..97108559hg19UCSC Ensembl
chr5:97030897..97134315hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38103419
hg19103419
hg18103419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598968, nsv598969
SamplesHGDP01399
Known GenesLOC102546227
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9938n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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